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Comparison · NCT01529268-9fdb3b7d

DR Cysteamine Bitartrate Capsule vs DR Cysteamine Bitartrate Placebo: Lobular Inflammation: Patients With Improvement

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. DR Cysteamine Bitartrate Capsule vs DR Cysteamine Bitartrate Placebo: Lobular Inflammation: Patients With Improvement. Trial comparisons, record NCT01529268-9fdb3b7d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01529268-9fdb3b7d

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3640.2710.468wilson
Risk in group 20.210.1350.311wilson
Risk difference, group 1 minus group 20.1540.01670.282newcombe hybrid score
Risk ratio, group 1 over group 21.731.052.87log
Odds ratio, group 1 over group 22.151.084.28log
Number needed to treat, for one more participant with the outcome on DR Cysteamine Bitartrate Capsule than on DR Cysteamine Bitartrate Placebo6.53.5559.8from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1DR Cysteamine Bitartrate Capsule
Active DR cysteamine bitartrate capsule~DR cysteamine bitartrate capsule: ◦ 600 mg/day (four 75 mg capsules twice daily) for patients ≤ 65 kg at baseline~* 750 mg/day (five 75 mg capsules twice daily) for patients \>65 - 80 kg at baseline~* 900 mg/day (six 75 mg capsules twice daily) for patients \>80 kg at baseline
3288OG000
Group 2DR Cysteamine Bitartrate Placebo
Placebo DR cysteamine bitartrate capsule~DR cysteamine bitartrate placebo: ◦ 600 mg/day (four 75 mg capsules twice daily) for patients ≤ 65 kg at baseline~* 750 mg/day (five 75 mg capsules twice daily) for patients \>65 - 80 kg at baseline~* 900 mg/day (six 75 mg capsules twice daily) for patients \>80 kg at baseline
1781OG001

Outcome

Type
SECONDARY
Title
Lobular Inflammation: Patients With Improvement
Description
Improvement in lobular inflammation defined as any decrease in lobular inflammation grade comparing 52-week biopsy to baseline.
Time frame
52 weeks
Population
Analysis based on intention to treat; patients with missing 52-week biopsy were imputed as lack of improvement.

Source ClinicalTrials.gov

Trial

Title
Cysteamine Bitartrate Delayed-Release for the Treatment of NAFLD in Children
NCT number
NCT01529268
Phases
PHASE2, PHASE3
Conditions
Nonalcoholic Fatty Liver Disease (NAFLD)
Interventions
DR cysteamine bitartrate capsule, DR cysteamine bitartrate placebo
Lead sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Results first posted
2017-09-05

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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